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Clinical metabolomics study on the intervention of hepatolenticular degeneration with Ganduling capsules

Clinical metabolomics study on the intervention of hepatolenticular degeneration with Ganduling capsules

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098794
Enrollment
Unknown
Registered
2025-03-13
Start date
2023-05-03
Completion date
Unknown
Last updated
2025-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wilson Disease

Interventions

Gandouling intervention group:The intervention group of Gandouling capsules on the basis of the HLD case-control group, liver douling capsules(0.3g/capsule, prepared by the Preparation Center of the F
control group:Conventional copper removal and hepatoprotective therapy

Sponsors

The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Complies with the diagnosis of hepatolenticular degeneration in accordance with the Chinese Guidelines for the Diagnosis and Treatment of Hepatolenticular Degeneration 2021; 2. Age range from 15 to 55 years old; 3. Avoid taking other traditional Chinese medicine or traditional Chinese patent medicines and simple preparations during the study period; 3. The patient or legal representative shall give informed consent and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Liver cirrhosis in the decompensated stage, manifested by portal hypertension, ascites, splenomegaly (WBC<3.0×10 9/L, PT<50×10 9), esophageal varices, gastrointestinal hemorrhage, moderate-to-severe anemia, or hepatic encephalopathy; 2. moderate-to-severe depression, recent suicidal thoughts or behavior, or severe psychiatric symptoms; 3. a history of severe seizures; 4. taking other Chinese medicines or proprietary Chinese medicines during the study period 5. patients who are unable to cooperate with the treatment.

Design outcomes

Primary

MeasureTime frame
Serum Copper;Ceruloplasmin;CoPPer oxidase;24-hour urine copper;

Secondary

MeasureTime frame
Blood routine;Liver function;

Countries

China

Contacts

Public ContactCao Shijian

The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine

626137134@qq.com+86 150 5624 8306

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026